Author

Rachel Slaugh

Washington University in St. LouisORCID 0000-0002-5742-9153Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:gene regulatory network inference· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Jennifer Ellen PoseyiD· 2 shared PATRICIA DICKSONiD· 2 shared 9P-ARCH· 1 shared Ahmet YeşilyurtiD· 1 shared Alison M. MuiriD· 1 shared Allan Micheil InnesiD· 1 shared Amber Neilson· 1 shared Amjad HoraniiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Jennifer Ellen PoseyORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineMolecular PsychiatryPeer-reviewedSep 16, 2026

DE NOVO VARIANTS IN THE POLY(RC)-BINDING PROTEIN GENE PCBP1 CAUSE A NEURODEVELOPMENTAL DISORDER

Wallid Deb, Thomas Besnard, Florence Desprez…·Sébastien Küry

The paper identifies de novo variants in PCBP1 causing neurodevelopmental disorders, showing impaired dendritic arborization and increased exon skipping in T cells.

DOI 10.1038/s41380-026-03877-w

humanbulk RNA-seq

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Genetic & Genomic MedicineGenome MedicinePeer-reviewedOct 24, 2025

Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p Syndromes

Yingxi Wang, Eleanor I. Sams, Rachel Slaugh…·Tychele N. Turner

This study uses whole-genome sequencing to analyze 9p deletion and duplication syndromes, identifying key genes and structural variants, and introduces a machine learning model for syndrome prediction.

7 citationstop 5%

humanwhole-genome sequencing

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